Perspectives on push–pull chromophores derived from click-type [2 + 2] cycloaddition–retroelectrocyclization reactions of electron-rich alkynes and electron-deficient alkenes
Various push–pull chromophores can be synthesized in a single and atom-economical step through [2 + 2] cycloaddition–retroelectrocyclization (CA–RE) reactions involving diverse electron-rich alkynes and electron-deficient alkenes. In this review, a comprehensive investigation of the recent and notew...
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Published in | Beilstein journal of organic chemistry Vol. 20; no. 1; pp. 125 - 154 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
Germany
Beilstein-Institut
22.01.2024
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Subjects | |
Online Access | Get full text |
ISSN | 1860-5397 1860-5397 |
DOI | 10.3762/bjoc.20.13 |
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Abstract | Various push–pull chromophores can be synthesized in a single and atom-economical step through [2 + 2] cycloaddition–retroelectrocyclization (CA–RE) reactions involving diverse electron-rich alkynes and electron-deficient alkenes. In this review, a comprehensive investigation of the recent and noteworthy advancements in the research on push–pull chromophores prepared via the [2 + 2] CA–RE reaction is conducted. In particular, an overview of the physicochemical properties of the family of these compounds that have been investigated is provided to clarify their potential for future applications. |
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AbstractList | Various push–pull chromophores can be synthesized in a single and atom-economical step through [2 + 2] cycloaddition–retroelectrocyclization (CA–RE) reactions involving diverse electron-rich alkynes and electron-deficient alkenes. In this review, a comprehensive investigation of the recent and noteworthy advancements in the research on push–pull chromophores prepared via the [2 + 2] CA–RE reaction is conducted. In particular, an overview of the physicochemical properties of the family of these compounds that have been investigated is provided to clarify their potential for future applications. |
Author | Yamada, Michio |
AuthorAffiliation | 1 Department of Chemistry, Tokyo Gakugei University, Nukuikitamachi 4-1-1, Koganei, Tokyo 184-8501, Japan https://ror.org/00khh5r84 https://www.isni.org/isni/0000000107205963 |
AuthorAffiliation_xml | – name: 1 Department of Chemistry, Tokyo Gakugei University, Nukuikitamachi 4-1-1, Koganei, Tokyo 184-8501, Japan https://ror.org/00khh5r84 https://www.isni.org/isni/0000000107205963 |
Author_xml | – sequence: 1 givenname: Michio orcidid: 0000-0002-6715-4202 surname: Yamada fullname: Yamada, Michio |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/38292046$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1021_acs_joc_4c02595 crossref_primary_10_1021_acs_joc_4c01328 crossref_primary_10_1002_chem_202404778 crossref_primary_10_1002_adsc_202400995 crossref_primary_10_1002_solr_202400803 crossref_primary_10_1002_asia_202401111 crossref_primary_10_1021_acsapm_4c02868 |
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Keywords | click chemistry photoinduced electron transfer donor–acceptor conjugate photoluminescence intramolecular charge transfer |
Language | English |
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Snippet | Various push–pull chromophores can be synthesized in a single and atom-economical step through [2 + 2] cycloaddition–retroelectrocyclization (CA–RE) reactions... Various push-pull chromophores can be synthesized in a single and atom-economical step through [2 + 2] cycloaddition-retroelectrocyclization (CA-RE) reactions... |
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SubjectTerms | Chemistry click chemistry donor–acceptor conjugate intramolecular charge transfer photoinduced electron transfer photoluminescence Review |
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Title | Perspectives on push–pull chromophores derived from click-type [2 + 2] cycloaddition–retroelectrocyclization reactions of electron-rich alkynes and electron-deficient alkenes |
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